The Recall Desk
Agency classClass IOur severity:SevereFDA (Drugs)·D-0935-2019·Announced 2019-03-20

King Bio Recalls NET Remedies Homeopathic Liquid Due to Microbial Contamination

King Bio Inc. is recalling NET Remedies #4 homeopathic liquid in the U.S., Canada, and Australia due to microbial contamination.

The agency’s classification

FDA (Drugs): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall is classified as FDA Class I, which meets the rubric criteria for a Severe rating.

Plain-English summary

King Bio Inc. is recalling 1,200 bottles of NET Remedies #4 (Green Label) Homeopathic Preparation, Oral Liquid, 57 mL. The product was distributed nationwide in the United States, as well as in Canada and Australia.

The recall was initiated due to microbial contamination. The affected lots are AUS-071718R with an expiration date of 07/20 and AUS-110117A with an expiration date of 11/19.

Consumers should stop using the product and contact the supplier or manufacturer for further instructions.

The recalled product

Product
NET Remedies #4 (Green Label) Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia
Manufacturer
King Bio Inc.
Affected units
1,200

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • Lots: AUS-071718R Exp. 07/20
  • AUS-110117A Exp. 11/19

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 465 recalled by King Bio Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 465 products in this recall →

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